Canonical Allele Identifier: CA2210542258

Gene: XYLT1

Linked Data

• dbSNP Id: rs2030854558

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.17138571_17138578del , CM000678.2:g.17138571_17138578del	GRCh38
NC_000016.9:g.17232428_17232435del , CM000678.1:g.17232428_17232435del	GRCh37
NC_000016.8:g.17139929_17139936del	NCBI36
NG_015843.1:g.337310_337317del
NG_015843.2:g.337310_337317del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261381.7:c.1588-41_1588-34del MANE Select	ENSP00000261381.6:n.1588-41_1588-34del
ENST00000261381.6:c.1588-41_1588-34del	ENSP00000261381.6:n.1588-41_1588-34del
NM_022166.3:c.1588-41_1588-34del	NP_071449.1:n.1588-41_1588-34del
XM_011522574.1:c.1588-41_1588-34del	XP_011520876.1:n.1588-41_1588-34del
XR_933141.1:n.504_511del
NR_135179.1:n.476_483del
XM_017023539.2:c.1588-41_1588-34del	XP_016879028.1:n.1588-41_1588-34del
XM_017023540.2:c.1588-41_1588-34del	XP_016879029.1:n.1588-41_1588-34del
NM_022166.4:c.1588-41_1588-34del MANE Select	NP_071449.1:n.1588-41_1588-34del